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First trimester combined screening for Trisomy 21 in Hong Kong: outcome of the first 10,000 cases
Objective. To examine the effectiveness of first trimester fetal Trisomy 21 (T21) screening using a combination of maternal age, nuchal translucency, maternal serum levels of free β-hCG and PAPP-A in a predominantly Chinese population in Hong Kong. Methods. Consecutive women who underwent the combin...
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Published in: | The journal of maternal-fetal & neonatal medicine 2009-01, Vol.22 (4), p.300-304 |
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container_title | The journal of maternal-fetal & neonatal medicine |
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creator | Leung, Tak Yeung Chan, Lin Wai Law, Lai Wa Sahota, Daljit Singh Fung, Tak Yuen Leung, Tse Ngong Lau, Tze Kin |
description | Objective. To examine the effectiveness of first trimester fetal Trisomy 21 (T21) screening using a combination of maternal age, nuchal translucency, maternal serum levels of free β-hCG and PAPP-A in a predominantly Chinese population in Hong Kong.
Methods. Consecutive women who underwent the combined screening for T21 between 11 and 13 + 6 weeks of gestation between 2003 and 2007 were recruited. Risk of T21 was calculated using Fetal Medicine Foundation algorithm and karyotyping was advised when the risk was 1:300 or above. All women were followed up for pregnancy and fetal outcome.
Results. 10,363 fetuses underwent screening. 99% of the women were Chinese and 27.4% were at or above 35 years old. 618 fetuses were screened positive (5.9%), which included 31 cases of T21, 14 cases of T18, 7 cases of T13, 10 cases of 45XO and 7 cases of other chromosomal abnormalities. Among the 9745 screened negative fetuses all but 50 (0.5%) had a known outcome, which included three T21 and four other chromosomal abnormalities. All were subsequently identified at the morphology scan except for one case of T21. The detection rate and false positive rates for T21 were 91.2% and 5.4%, respectively and the positive predictive value for all chromosomal abnormalities was 1 in 9.
Conclusions. Combined screening for T21 is highly effective among Chinese women. Training, quality control, regular auditing and follow up are essential to maintain screening standards. |
doi_str_mv | 10.1080/14767050802430842 |
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Methods. Consecutive women who underwent the combined screening for T21 between 11 and 13 + 6 weeks of gestation between 2003 and 2007 were recruited. Risk of T21 was calculated using Fetal Medicine Foundation algorithm and karyotyping was advised when the risk was 1:300 or above. All women were followed up for pregnancy and fetal outcome.
Results. 10,363 fetuses underwent screening. 99% of the women were Chinese and 27.4% were at or above 35 years old. 618 fetuses were screened positive (5.9%), which included 31 cases of T21, 14 cases of T18, 7 cases of T13, 10 cases of 45XO and 7 cases of other chromosomal abnormalities. Among the 9745 screened negative fetuses all but 50 (0.5%) had a known outcome, which included three T21 and four other chromosomal abnormalities. All were subsequently identified at the morphology scan except for one case of T21. The detection rate and false positive rates for T21 were 91.2% and 5.4%, respectively and the positive predictive value for all chromosomal abnormalities was 1 in 9.
Conclusions. Combined screening for T21 is highly effective among Chinese women. Training, quality control, regular auditing and follow up are essential to maintain screening standards.</description><identifier>ISSN: 1476-7058</identifier><identifier>EISSN: 1476-4954</identifier><identifier>DOI: 10.1080/14767050802430842</identifier><identifier>PMID: 19085637</identifier><language>eng</language><publisher>England: Informa UK Ltd</publisher><subject>Adult ; Asian Continental Ancestry Group ; Chinese ; Down Syndrome - diagnosis ; Female ; free β-human chorionic gonadotropin ; Genetic Testing ; Hong Kong ; Humans ; nuchal translucency ; Predictive Value of Tests ; Pregnancy ; pregnancy associated plasma protein A ; Pregnancy Trimester, First ; Prenatal Diagnosis ; Prospective Studies ; screening ; Trisomy 21</subject><ispartof>The journal of maternal-fetal & neonatal medicine, 2009-01, Vol.22 (4), p.300-304</ispartof><rights>2009 Informa UK Ltd All rights reserved: reproduction in whole or part not permitted 2009</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c404t-8686f009a7918ce619e00065f6241c33f62b66a91261bc51dd944545a66d1c213</citedby><cites>FETCH-LOGICAL-c404t-8686f009a7918ce619e00065f6241c33f62b66a91261bc51dd944545a66d1c213</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19085637$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Leung, Tak Yeung</creatorcontrib><creatorcontrib>Chan, Lin Wai</creatorcontrib><creatorcontrib>Law, Lai Wa</creatorcontrib><creatorcontrib>Sahota, Daljit Singh</creatorcontrib><creatorcontrib>Fung, Tak Yuen</creatorcontrib><creatorcontrib>Leung, Tse Ngong</creatorcontrib><creatorcontrib>Lau, Tze Kin</creatorcontrib><title>First trimester combined screening for Trisomy 21 in Hong Kong: outcome of the first 10,000 cases</title><title>The journal of maternal-fetal & neonatal medicine</title><addtitle>J Matern Fetal Neonatal Med</addtitle><description>Objective. To examine the effectiveness of first trimester fetal Trisomy 21 (T21) screening using a combination of maternal age, nuchal translucency, maternal serum levels of free β-hCG and PAPP-A in a predominantly Chinese population in Hong Kong.
Methods. Consecutive women who underwent the combined screening for T21 between 11 and 13 + 6 weeks of gestation between 2003 and 2007 were recruited. Risk of T21 was calculated using Fetal Medicine Foundation algorithm and karyotyping was advised when the risk was 1:300 or above. All women were followed up for pregnancy and fetal outcome.
Results. 10,363 fetuses underwent screening. 99% of the women were Chinese and 27.4% were at or above 35 years old. 618 fetuses were screened positive (5.9%), which included 31 cases of T21, 14 cases of T18, 7 cases of T13, 10 cases of 45XO and 7 cases of other chromosomal abnormalities. Among the 9745 screened negative fetuses all but 50 (0.5%) had a known outcome, which included three T21 and four other chromosomal abnormalities. All were subsequently identified at the morphology scan except for one case of T21. The detection rate and false positive rates for T21 were 91.2% and 5.4%, respectively and the positive predictive value for all chromosomal abnormalities was 1 in 9.
Conclusions. Combined screening for T21 is highly effective among Chinese women. Training, quality control, regular auditing and follow up are essential to maintain screening standards.</description><subject>Adult</subject><subject>Asian Continental Ancestry Group</subject><subject>Chinese</subject><subject>Down Syndrome - diagnosis</subject><subject>Female</subject><subject>free β-human chorionic gonadotropin</subject><subject>Genetic Testing</subject><subject>Hong Kong</subject><subject>Humans</subject><subject>nuchal translucency</subject><subject>Predictive Value of Tests</subject><subject>Pregnancy</subject><subject>pregnancy associated plasma protein A</subject><subject>Pregnancy Trimester, First</subject><subject>Prenatal Diagnosis</subject><subject>Prospective Studies</subject><subject>screening</subject><subject>Trisomy 21</subject><issn>1476-7058</issn><issn>1476-4954</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><recordid>eNp9kE9LxDAQxYMo_v8AXiQnT67OtEnaqhcRV0XBi55DNp26kbbRpEX22xvdBRHBy8wwvPeY-TF2gHCCUMIpikIVINOYiRxKka2x7a_dRFRSrK_mJCi32E6MrwAZCpCbbAsrKKXKi21mpi7EgQ_BdRQHCtz6buZ6qnm0gah3_QtvfOBPwUXfLXiG3PX81qf1fSpn3I9DshD3DR_mxJvvOIRjAODWRIp7bKMxbaT9Vd9lz9Prp6vbycPjzd3V5cPEChDDpFSlagAqU1RYWlJYUYpQslGZQJvnqc-UMhVmCmdWYl1XQkghjVI12gzzXXa0zH0L_n1Mz-jORUtta3ryY9SqwKKQpUhCXApt8DEGavRb-t6EhUbQX1z1H67Jc7gKH2cd1T-OFcgkuFgKXJ9wdebDh7bWg1m0PjTB9NZFnf-Xf_7LPifTDnNrAulXP4Y-gfvnuk8SPJUz</recordid><startdate>20090101</startdate><enddate>20090101</enddate><creator>Leung, Tak Yeung</creator><creator>Chan, Lin Wai</creator><creator>Law, Lai Wa</creator><creator>Sahota, Daljit Singh</creator><creator>Fung, Tak Yuen</creator><creator>Leung, Tse Ngong</creator><creator>Lau, Tze Kin</creator><general>Informa UK Ltd</general><general>Taylor & Francis</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20090101</creationdate><title>First trimester combined screening for Trisomy 21 in Hong Kong: outcome of the first 10,000 cases</title><author>Leung, Tak Yeung ; Chan, Lin Wai ; Law, Lai Wa ; Sahota, Daljit Singh ; Fung, Tak Yuen ; Leung, Tse Ngong ; Lau, Tze Kin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c404t-8686f009a7918ce619e00065f6241c33f62b66a91261bc51dd944545a66d1c213</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Adult</topic><topic>Asian Continental Ancestry Group</topic><topic>Chinese</topic><topic>Down Syndrome - diagnosis</topic><topic>Female</topic><topic>free β-human chorionic gonadotropin</topic><topic>Genetic Testing</topic><topic>Hong Kong</topic><topic>Humans</topic><topic>nuchal translucency</topic><topic>Predictive Value of Tests</topic><topic>Pregnancy</topic><topic>pregnancy associated plasma protein A</topic><topic>Pregnancy Trimester, First</topic><topic>Prenatal Diagnosis</topic><topic>Prospective Studies</topic><topic>screening</topic><topic>Trisomy 21</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Leung, Tak Yeung</creatorcontrib><creatorcontrib>Chan, Lin Wai</creatorcontrib><creatorcontrib>Law, Lai Wa</creatorcontrib><creatorcontrib>Sahota, Daljit Singh</creatorcontrib><creatorcontrib>Fung, Tak Yuen</creatorcontrib><creatorcontrib>Leung, Tse Ngong</creatorcontrib><creatorcontrib>Lau, Tze Kin</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>The journal of maternal-fetal & neonatal medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Leung, Tak Yeung</au><au>Chan, Lin Wai</au><au>Law, Lai Wa</au><au>Sahota, Daljit Singh</au><au>Fung, Tak Yuen</au><au>Leung, Tse Ngong</au><au>Lau, Tze Kin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>First trimester combined screening for Trisomy 21 in Hong Kong: outcome of the first 10,000 cases</atitle><jtitle>The journal of maternal-fetal & neonatal medicine</jtitle><addtitle>J Matern Fetal Neonatal Med</addtitle><date>2009-01-01</date><risdate>2009</risdate><volume>22</volume><issue>4</issue><spage>300</spage><epage>304</epage><pages>300-304</pages><issn>1476-7058</issn><eissn>1476-4954</eissn><abstract>Objective. To examine the effectiveness of first trimester fetal Trisomy 21 (T21) screening using a combination of maternal age, nuchal translucency, maternal serum levels of free β-hCG and PAPP-A in a predominantly Chinese population in Hong Kong.
Methods. Consecutive women who underwent the combined screening for T21 between 11 and 13 + 6 weeks of gestation between 2003 and 2007 were recruited. Risk of T21 was calculated using Fetal Medicine Foundation algorithm and karyotyping was advised when the risk was 1:300 or above. All women were followed up for pregnancy and fetal outcome.
Results. 10,363 fetuses underwent screening. 99% of the women were Chinese and 27.4% were at or above 35 years old. 618 fetuses were screened positive (5.9%), which included 31 cases of T21, 14 cases of T18, 7 cases of T13, 10 cases of 45XO and 7 cases of other chromosomal abnormalities. Among the 9745 screened negative fetuses all but 50 (0.5%) had a known outcome, which included three T21 and four other chromosomal abnormalities. All were subsequently identified at the morphology scan except for one case of T21. The detection rate and false positive rates for T21 were 91.2% and 5.4%, respectively and the positive predictive value for all chromosomal abnormalities was 1 in 9.
Conclusions. Combined screening for T21 is highly effective among Chinese women. Training, quality control, regular auditing and follow up are essential to maintain screening standards.</abstract><cop>England</cop><pub>Informa UK Ltd</pub><pmid>19085637</pmid><doi>10.1080/14767050802430842</doi><tpages>5</tpages></addata></record> |
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source | Taylor and Francis:Jisc Collections:Taylor and Francis Read and Publish Agreement 2024-2025:Medical Collection (Reading list) |
subjects | Adult Asian Continental Ancestry Group Chinese Down Syndrome - diagnosis Female free β-human chorionic gonadotropin Genetic Testing Hong Kong Humans nuchal translucency Predictive Value of Tests Pregnancy pregnancy associated plasma protein A Pregnancy Trimester, First Prenatal Diagnosis Prospective Studies screening Trisomy 21 |
title | First trimester combined screening for Trisomy 21 in Hong Kong: outcome of the first 10,000 cases |
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